NP-MRD: Showing NP-Card for Gibberellin A1 glucosyl ester (NP0337409)

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Record Information

Version

2.0

Created at

2024-09-11 10:43:50 UTC

Updated at

2024-09-11 10:43:51 UTC

NP-MRD ID

NP0337409

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Gibberellin A1 glucosyl ester

Description

Not Available

Structure

MOL SDF PDB SMILES InChI


  Mrv1652307292023442D          

 38 43  0  0  1  0            999 V2000
    0.1402   -0.5591    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0861    0.9376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3767    1.5712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1399    1.8842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1453    0.7794    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8608    1.4823    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4440    0.0553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6203    0.1046    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3958   -1.3435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2032   -1.5143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6433    1.3426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8031   -0.0720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3659   -1.5436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1984    0.0230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6433   -1.1253    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1144   -0.0036    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3594    0.9318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0739    0.5193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0739   -0.3058    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3594   -0.7181    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6449   -0.3058    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6449    0.5193    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7884   -0.7183    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9958    0.6683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5591   -4.0195    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2736   -4.4320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1552   -4.4320    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1552   -5.2570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8697   -4.0195    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1552   -2.7820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1553   -1.9571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2736   -2.7821    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8697   -3.1945    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5592   -3.1945    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5842   -4.4320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5842   -5.2570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7876    0.4369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5354    1.9571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  4  6  1  0  0  0  0
  5  8  1  0  0  0  0
  7  8  1  0  0  0  0
  8  2  1  6  0  0  0
  6  2  1  6  0  0  0
  1  8  1  0  0  0  0
  1  9  1  1  0  0  0
  9 10  2  0  0  0  0
 11 12  1  0  0  0  0
 12 14  2  0  0  0  0
  5 16  1  1  0  0  0
 17 18  1  0  0  0  0
 17 22  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 11  1  6  0  0  0
 22  5  1  0  0  0  0
 21 15  1  1  0  0  0
 21  1  1  0  0  0  0
 20 13  1  0  0  0  0
 20 12  1  6  0  0  0
 19 23  1  1  0  0  0
  6 24  1  0  0  0  0
  7 24  1  0  0  0  0
 29 27  1  0  0  0  0
 29 33  1  0  0  0  0
 27 25  1  0  0  0  0
 33 30  1  0  0  0  0
 25 34  1  0  0  0  0
 30 34  1  0  0  0  0
 25 26  1  1  0  0  0
 27 28  1  6  0  0  0
 29 35  1  1  0  0  0
 30 31  1  1  0  0  0
 34 32  1  6  0  0  0
 35 36  1  0  0  0  0
 24 37  2  0  0  0  0
  6 38  1  0  0  0  0
  9 31  1  0  0  0  0
M  END


  Mrv1652307292023442D          

 38 43  0  0  1  0            999 V2000
    0.1402   -0.5591    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0861    0.9376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3767    1.5712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1399    1.8842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1453    0.7794    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8608    1.4823    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4440    0.0553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6203    0.1046    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3958   -1.3435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2032   -1.5143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6433    1.3426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8031   -0.0720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3659   -1.5436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1984    0.0230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6433   -1.1253    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1144   -0.0036    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3594    0.9318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0739    0.5193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0739   -0.3058    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3594   -0.7181    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6449   -0.3058    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6449    0.5193    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7884   -0.7183    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9958    0.6683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5591   -4.0195    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2736   -4.4320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1552   -4.4320    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1552   -5.2570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8697   -4.0195    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1552   -2.7820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1553   -1.9571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2736   -2.7821    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8697   -3.1945    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5592   -3.1945    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5842   -4.4320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5842   -5.2570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7876    0.4369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5354    1.9571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  4  6  1  0  0  0  0
  5  8  1  0  0  0  0
  7  8  1  0  0  0  0
  8  2  1  6  0  0  0
  6  2  1  6  0  0  0
  1  8  1  0  0  0  0
  1  9  1  1  0  0  0
  9 10  2  0  0  0  0
 11 12  1  0  0  0  0
 12 14  2  0  0  0  0
  5 16  1  1  0  0  0
 17 18  1  0  0  0  0
 17 22  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 11  1  6  0  0  0
 22  5  1  0  0  0  0
 21 15  1  1  0  0  0
 21  1  1  0  0  0  0
 20 13  1  0  0  0  0
 20 12  1  6  0  0  0
 19 23  1  1  0  0  0
  6 24  1  0  0  0  0
  7 24  1  0  0  0  0
 29 27  1  0  0  0  0
 29 33  1  0  0  0  0
 27 25  1  0  0  0  0
 33 30  1  0  0  0  0
 25 34  1  0  0  0  0
 30 34  1  0  0  0  0
 25 26  1  1  0  0  0
 27 28  1  6  0  0  0
 29 35  1  1  0  0  0
 30 31  1  1  0  0  0
 34 32  1  6  0  0  0
 35 36  1  0  0  0  0
 24 37  2  0  0  0  0
  6 38  1  0  0  0  0
  9 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0337409

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12CC[C@]3(O)C[C@]1(CC3=C)[C@@H](C(=O)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)[C@]1([H])[C@@]3(C)[C@@H](O)CC[C@@]21OC3=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H34O11/c1-10-7-23-9-24(10,33)5-3-12(23)25-6-4-13(27)22(2,21(32)36-25)18(25)14(23)19(31)35-20-17(30)16(29)15(28)11(8-26)34-20/h11-18,20,26-30,33H,1,3-9H2,2H3/t11-,12-,13+,14-,15-,16+,17-,18-,20+,22-,23+,24+,25-/m1/s1

> <INCHI_KEY>
YNUHPGJFLBSPMR-HRHVLVCKSA-N

> <FORMULA>
C25H34O11

> <MOLECULAR_WEIGHT>
510.5309

> <EXACT_MASS>
510.21011193

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
51.24088107274048

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (1R,2R,5S,8S,9S,10R,11S,12S)-5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane-9-carboxylate

> <ALOGPS_LOGP>
-1.05

> <JCHEM_LOGP>
-1.8670480730000003

> <ALOGPS_LOGS>
-1.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.173257870417391

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.193705794965876

> <JCHEM_PKA_STRONGEST_BASIC>
-0.904784152979622

> <JCHEM_POLAR_SURFACE_AREA>
183.20999999999998

> <JCHEM_REFRACTIVITY>
118.03809999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.89e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (1R,2R,5S,8S,9S,10R,11S,12S)-5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane-9-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-JUL-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-JUL-20         0                                  
HETATM    1  C   UNK     0       0.262  -1.044   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.027   1.750   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.703   2.933   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.128   3.517   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.271   1.455   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.473   2.767   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.695   0.103   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.158   0.195   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.739  -2.508   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.246  -2.827   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      -1.201   2.506   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -3.366  -0.134   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.550  -2.881   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -2.237   0.043   0.000  0.00  0.00           O+0
HETATM   15  H   UNK     0      -1.201  -2.101   0.000  0.00  0.00           H+0
HETATM   16  H   UNK     0      -0.214  -0.007   0.000  0.00  0.00           H+0
HETATM   17  C   UNK     0      -2.538   1.739   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.871   0.969   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.871  -0.571   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.538  -1.340   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.204  -0.571   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.204   0.969   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -5.205  -1.341   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.725   1.247   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.044  -7.503   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.377  -8.273   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -0.290  -8.273   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -0.290  -9.813   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -1.623  -7.503   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.290  -5.193   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -0.290  -3.653   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       2.377  -5.193   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      -1.623  -5.963   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       1.044  -5.963   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -2.957  -8.273   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -2.957  -9.813   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       5.204   0.816   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       4.733   3.653   0.000  0.00  0.00           O+0
CONECT    1    8    9   21                                                  
CONECT    2    8    6                                                       
CONECT    3    4    5                                                       
CONECT    4    3    6                                                       
CONECT    5    3    8   16   22                                             
CONECT    6    4    2   24   38                                             
CONECT    7    8   24                                                       
CONECT    8    5    7    2    1                                             
CONECT    9    1   10   31                                                  
CONECT   10    9                                                            
CONECT   11   12   22                                                       
CONECT   12   11   14   20                                                  
CONECT   13   20                                                            
CONECT   14   12                                                            
CONECT   15   21                                                            
CONECT   16    5                                                            
CONECT   17   18   22                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   23                                                  
CONECT   20   19   21   13   12                                             
CONECT   21   20   22   15    1                                             
CONECT   22   17   21   11    5                                             
CONECT   23   19                                                            
CONECT   24    6    7   37                                                  
CONECT   25   27   34   26                                                  
CONECT   26   25                                                            
CONECT   27   29   25   28                                                  
CONECT   28   27                                                            
CONECT   29   27   33   35                                                  
CONECT   30   33   34   31                                                  
CONECT   31   30    9                                                       
CONECT   32   34                                                            
CONECT   33   29   30                                                       
CONECT   34   25   30   32                                                  
CONECT   35   29   36                                                       
CONECT   36   35                                                            
CONECT   37   24                                                            
CONECT   38    6                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   86    0
END

View in JSmol

Synonyms

Value	Source
Gibberellin A1 glucosyl ester	HMDB
GA1 glucosyl ester	HMDB

Chemical Formula

C₂₅H₃₄O₁₁

Average Mass

510.5309 Da

Monoisotopic Mass

510.21011 Da

IUPAC Name

(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (1R,2R,5S,8S,9S,10R,11S,12S)-5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane-9-carboxylate

Traditional Name

CAS Registry Number

Not Available

SMILES

[H][C@@]12CC[C@]3(O)C[C@]1(CC3=C)[C@@H](C(=O)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)[C@]1([H])[C@@]3(C)[C@@H](O)CC[C@@]21OC3=O

InChI Identifier

InChI=1S/C25H34O11/c1-10-7-23-9-24(10,33)5-3-12(23)25-6-4-13(27)22(2,21(32)36-25)18(25)14(23)19(31)35-20-17(30)16(29)15(28)11(8-26)34-20/h11-18,20,26-30,33H,1,3-9H2,2H3/t11-,12-,13+,14-,15-,16+,17-,18-,20+,22-,23+,24+,25-/m1/s1

InChI Key

YNUHPGJFLBSPMR-HRHVLVCKSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Cyclic alpha peptide
Phenylalanine or derivatives
Macrolactam
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
Alpha-amino acid or derivatives
Amphetamine or derivatives
N-acylpyrrolidine
Anisole
Aralkylamine
Alkyl aryl ether
Fatty acyl
Benzenoid
Fatty amide
Monocyclic benzene moiety
Tertiary carboxylic acid amide
Pyrrolidine
Tertiary amine
Carboxamide group
Amino acid or derivatives
Lactam
Tertiary aliphatic amine
Secondary carboxylic acid amide
Azacycle
Oxacycle
Ether
Organoheterocyclic compound
Organic nitrogen compound
Carbonyl group
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Amine
Organopnictogen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	-1	ALOGPS
logP	-1.9	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	12.19	ChemAxon
pKa (Strongest Basic)	-0.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	183.21 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	118.04 m³·mol⁻¹	ChemAxon
Polarizability	51.24 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0038609

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB018000

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Gibberellin A1 glucosyl ester (NP0337409)

MOL for NP0337409 (Gibberellin A1 glucosyl ester)

3D MOL for NP0337409 (Gibberellin A1 glucosyl ester)

3D SDF for NP0337409 (Gibberellin A1 glucosyl ester)

3D-SDF for NP0337409 (Gibberellin A1 glucosyl ester)

PDB for NP0337409 (Gibberellin A1 glucosyl ester)

3D PDB for NP0337409 (Gibberellin A1 glucosyl ester)

SMILES for NP0337409 (Gibberellin A1 glucosyl ester)

INCHI for NP0337409 (Gibberellin A1 glucosyl ester)

Structure for NP0337409 (Gibberellin A1 glucosyl ester)

3D Structure for NP0337409 (Gibberellin A1 glucosyl ester)